Linked Data
MyVariant Identifiers:
chr1:g.115256489T>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.114713868T>G , CM000663.2:g.114713868T>G | GRCh38 |
| NC_000001.10:g.115256489T>G , CM000663.1:g.115256489T>G | GRCh37 |
| NC_000001.9:g.115058012T>G | NCBI36 |
| NG_007572.1:g.8027A>C , LRG_92:g.8027A>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369535.5:c.222A>C MANE Select | ENSP00000358548.4:p.Thr74= | |
| ENST00000369535.4:c.222A>C | ENSP00000358548.4:p.Thr74= | |
| NM_002524.4:c.222A>C | NP_002515.1:p.Thr74= | |
| NM_002524.5:c.222A>C MANE Select | NP_002515.1:p.Thr74= |